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Sigma-Aldrich

Tetrakis(pyridine)copper(II) triflate

95%

Synonym(s):

[Cu(OTf)2(py)4], Cu(pyridine)4(OTf)2, Tetrakis(pyridine)copper(II) bis(trifluoromethanesulfonate)

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About This Item

Empirical Formula (Hill Notation):
C22H20CuF6N4O6S2
CAS Number:
113110-58-0
Molecular Weight:
678.08
UNSPSC Code:
12352300
PubChem Substance ID:
329764907

Quality Level

100

Assay

95%

form

crystals

reaction suitability

core: copper
reagent type: catalyst

mp

190-194 °C

storage temp.

−20°C

SMILES string

c1ccncc1.c2ccncc2.c3ccncc3.c4ccncc4.FC(F)(F)S(=O)(=O)O[Cu]OS(=O)(=O)C(F)(F)F

InChI

1S/4C5H5N.2CHF3O3S.Cu/c4*1-2-4-6-5-3-1;2*2-1(3,4)8(5,6)7;/h4*1-5H;2*(H,5,6,7);/q;;;;;;+2/p-2

InChI key

DOUMBTAZXRQKGF-UHFFFAOYSA-L

Related Categories

Application

Tetrakis(pyridine)copper(II) triflate [Cu(OTf)2(py)4] is a general copper-based catalyst. It is commonly used to catalyze copper-mediated radiofluorination of arenes and heteroarene. It is also employed in C(sp3)-H functionalization/cyclisation of 2-amino-N,N-dialkylbenzamides to synthesize 2,3-disubstituted-4(3H)-quinazolinones.
Tetrakis(pyridine)copper(II) triflate can be used to catalyze:
  • Intra and intermolecular aziridination of allylic carbamates and styrenes.
  • 18F-fluorination of aryl boronic esters to generate fluroarenes applicable as radiotracers.
  • Nucleophilic radiobromination of aryl borons with a radiobromide ion applicable in the preparation of radiobrominated pharmaceuticals.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Skin Corr. 1B

Storage Class Code

8A - Combustible, corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Preparation of No?Carrier?Added 6?[18F] Fluoro?l?tryptophan via Cu?Mediated Radiofluorination.
Schafer D, et al.
European Journal of Organic Chemistry, 2016(27), 4621-4628 (2016)
Copper-catalyzed alkene aziridination with N-tosyloxycarbamates
Lebel H, et al.
Organic Letters, 9(23), 4797-4800 (2007)
Copper-catalyzed C?H functionalization reactions: Efficient synthesis of heterocycles.
Guo X X, et al.
Chemical Reviews, 115(3), 1622-1651 (2014)
Copper-mediated nucleophilic radiobromination of aryl boron precursors: Convenient preparation of a radiobrominated PARP-1 inhibitor
Zhou D, et al.
Tetrahedron Letters, 59(20), 1963-1967 (2018)
Synthesis of Cu-catalysed quinazolinones using a C sp3?H functionalisation/cyclisation strategy.
Gholap A V, et al.
Organic & Biomolecular Chemistry, 15(34), 7140-7146 (2017)
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